Canonical Allele Identifier: CA2269946090

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488967_63488968delinsAG , CM000679.2:g.63488967_63488968delinsAG	GRCh38
NC_000017.10:g.61566328_61566329delinsAG , CM000679.1:g.61566328_61566329delinsAG	GRCh37
NC_000017.9:g.58920060_58920061delinsAG	NCBI36
NG_011648.1:g.16895_16896delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2476_2477delinsAG MANE Select	ENSP00000290866.4:p.Arg826=
ENST00000290863.10:c.754_755delinsAG	ENSP00000290863.6:p.Arg252=
ENST00000290866.9:c.2476_2477delinsAG	ENSP00000290866.4:p.Arg826=
ENST00000413513.7:c.754_755delinsAG	ENSP00000392247.3:p.Arg252=
ENST00000428043.5:c.2476_2477delinsAG	ENSP00000397593.2:p.Arg826=
ENST00000577647.2:c.754_755delinsAG	ENSP00000464149.1:p.Arg252=
ENST00000578839.5:c.*519+176_*519+177delinsAG	ENSP00000462110.2:n.*519+176_*519+177delinsAG
ENST00000579204.1:c.735_736delinsAG	ENSP00000464629.1:n.735_736delinsAG
ENST00000579314.5:c.*205_*206delinsAG	ENSP00000462599.1:n.*205_*206delinsAG
ENST00000582005.5:c.*396_*397delinsAG	ENSP00000462002.1:n.*396_*397delinsAG
ENST00000582761.1:c.244_245delinsAG	ENSP00000462909.1:p.Arg82=
ENST00000584865.5:n.422_423delinsAG
NM_000789.3:c.2476_2477delinsAG	NP_000780.1:p.Arg826=
NM_001178057.1:c.754_755delinsAG	NP_001171528.1:p.Arg252=
NM_152830.2:c.754_755delinsAG	NP_690043.1:p.Arg252=
XM_005257110.1:c.1927_1928delinsAG	XP_005257167.1:p.Arg643=
XM_006721737.2:c.814_815delinsAG	XP_006721800.2:p.Arg272=
XM_006721737.3:c.814_815delinsAG	XP_006721800.2:p.Arg272=
NM_000789.4:c.2476_2477delinsAG MANE Select	NP_000780.1:p.Arg826=
NM_001178057.2:c.754_755delinsAG	NP_001171528.1:p.Arg252=
NM_152830.3:c.754_755delinsAG	NP_690043.1:p.Arg252=
NM_001382700.1:c.1909_1910delinsAG	NP_001369629.1:p.Arg637=
NM_001382701.1:c.1624_1625delinsAG	NP_001369630.1:p.Arg542=
NM_001382702.1:c.379+176_379+177delinsAG	NP_001369631.1:n.379+176_379+177delinsAG
NR_168483.1:n.854_855delinsAG